@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_head
{
this:
np:hasAssertion
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_assertion
;
np:hasProvenance
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_provenance
;
np:hasPublicationInfo
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_assertion
a
np:Assertion
.
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_provenance
a
np:Provenance
.
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_assertion
{
miriam-gene:3492
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNd5079d4ae9f285d663edb230d71c70b8
sio:SIO_000628
miriam-gene:3492
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_provenance
{
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_assertion
dcterms:description
"[Molecular diagnostic laboratories face such difficulties with the BCL2-IGH translocation in follicular lymphoma and with internal tandem duplication mutation of the FLT3 gene in leukemia, where breakpoints are widely distributed, mutations may be multiple, signal strength is low, and background noise is elevated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21227398
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP620016.RA1DtZTGXJf5GJP2os7YbINp_nVzh0r4mcMZZQjUJCmt4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}